scholarly journals Thallium Associated with Manganese Ore Tailings in a Deactivated Mine in the Western Region of Bahia, Brazil

Author(s):  
Jorge Luís Santos ◽  
Giuliana Bueno ◽  
Eder Flores ◽  
Oldair Leite ◽  
Clayton Janoni ◽  
...  

Thallium (Tl) is a rare metal with toxic effects notably harmful to human health and the environment. In this article, the natural occurrence of Tl was evaluated in a deactivated manganese mine located in the Western region of Bahia, Brazil. The extraction procedure with aqua regia was used to dissolve the soil, sediment, and tailings samples. The Tl content was determined by differential pulse anodic stripping voltammetry (DPASV) and manganese (Mn) and iron (Fe) by flame atomic absorption spectroscopy (FAAS). The Tl levels ranged from 0.64 to 473 mg kg‑1, triggering an alert since most of the samples (soil and sediment) analyzed presented Tl concentrations above 1.0 mg kg-1, recognized as the maximum limit recommended by environmental agencies in North America and Europe.

1977 ◽  
Vol 12 (1) ◽  
pp. 157-178 ◽  
Author(s):  
P.M. Stokes ◽  
A.M. Szokalo

Abstract Lake and stream sediments often reflect recent additions of heavy metals before elevations of such elements are detectable in the overlying water. Concentrations of metals in sediments of lakes may be three to four orders of magnitude greater than in the water. While tests of water quality may, therefore, indicate no elevated metal levels in the soluble phase, a water body may still be heavily polluted, with organic and inorganic material in sediments acting as sites for precipitation and adsorption of the metals. The possibility of reentry of sedimented material into the water, due to physical, chemical or biological processes in natural situations, always exists. Experimental work was carried out on nickel and copper in the sediments of Middle Lake (recently limed to pH 6.5, and fertilized) and of Clearwater Lake (untreated), Sudbury, Ontario, under a variety of physical and biological conditions in aquaria. Results showed that both copper and nickel increased in concentration in water overlying the sediments, eg. in “live” aerobic systems over 28 days total copper in water increased from 0.15 to 0.85 ppm, and total nickel from 0.3 to 3.0 ppm. The pH of the water, initially 6.5, dropped to below 4.0. In sterile anaerobic conditions, total copper decreased slightly, and total nickel remained constant, while pH in this condition initially dropped only slightly, and at 28 days was 6.0. The “live” anaerobic system was intermediate in all these respects. “Free” copper at lower pH values (measured by differential pulse anodic stripping voltammetry) was predictably equal to total copper (measured by flame atomic absorption or by anodic stripping), but in the sterile anaerobic treatments where pH was 6.0, “free” copper was less than 50% of the total copper. Since ionic copper is believed to be the form toxic to biota, the lowered pH and increased ionic copper in water close to the sediments appears to have serious implications.


2019 ◽  
Vol 63 (1) ◽  
Author(s):  
Mehdi Jalali ◽  
Zeinab Deris Falahieh ◽  
Mohammad Alimoradi ◽  
Jalal Albadi ◽  
Ali Niazi

The electrochemical behavior of Bi+3 ions on the surface of a glassy carbon electrode, in acidic media and in the presence of tamoxifen, was investigated. Cyclic voltammetry, chronoamperometry, differential pulse voltammetry, electrochemical impedance spectroscopy, and scanning electron microscopy with energy-dispersive X-ray spectroscopy were used to find the probable mechanism contributing to the reduction of the peak height of bismuth oxidation with an increase in the concentration of tamoxifen. The obtained results show a slight interaction between the bismuth species and tamoxifen which co-deposit on the surface of glassy carbon electrode. Therefore, the reduction in the peak height of bismuth oxidation as a function of tamoxifen concentration was used to develop a new differential pulse anodic striping voltammetry method for determination of trace amount of tamoxifen. The effects of experimental parameters on the in situ DPASV of Bi+3 ions in the presence of tamoxifen shown the optimal conditions as: 2 mol L-1 H2SO4 (1% v v-1 MeOH), a deposition potential of -0.5 V, a deposition time of 60 s, and a glassy carbon electrode rotation rate of 300 rpm. The calibration curve was plotted in the range of 0.5 to 6 µg mL-1 and the limits of detection and quantitation were calculated to be 3.1 × 10-5 µg mL-1 and 1.0 × 10-4 µg mL-1, respectively. The mean, RSD, and relative bias for 0.5 µg mL-1 (n=5) were found to be 0.49 µg mL-1, 0.3%, and 2%, respectively. Finally, the proposed method was successfully used for the determination of tamoxifen in serum and pharmaceutical samples.


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